Hypodermic Needles, Single Lumen
FDA 510(k) K874414 · Harbor Medical Devices, Inc.
510(k) numberK874414
Submission
- Device name
- Hypodermic Needles, Single Lumen
- Applicant
- Harbor Medical Devices, Inc.
Boston, MA, US - Received
- October 28, 1987
- Decision date
- January 14, 1988
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- FMI – Needle, Hypodermic, Single Lumen
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5570
- Specialty
- General Hospital
Other 510(k)s with product code FMI
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261719 | Promisemed X-Safety Pen NeedleFMI · Special | Promisemed Hangzhou Meditech Co., Ltd. | 08/25/2026SE |
| K262427 | Pen Needle (Ordinary Type I, Safety Type IIA, Safety Type IIB, Safety Type IIIA, Safety…FMI · Special | Hh Global Technology, Inc. | 08/10/2026SE |
| K260933 | Safety Sterile Hypodermic Needles (NR-S1816R, NR-S1916R, NR-S1925R, NR-S1938R…FMI · Traditional | Hangzhou Qiantang Longyue Biotechnology Co., Ltd. | 08/07/2026SE |
| K261829 | Profoject Dual-Safety Pen NeedlesFMI · Traditional | CMT Health PTE., Ltd. | 07/29/2026SE |
| K260739 | Profoject Pen Needles (Model A; Model B)FMI · Traditional | CMT Health PTE., Ltd. | 07/15/2026SE |
| K260855 | Profoject Safety Pen NeedlesFMI · Traditional | CMT Health PTE., Ltd. | 06/10/2026SE |
| K254273 | Verisafe Safety Sterile Needles (SSN)FMI · Special | Promisemed Hangzhou Meditech Co., Ltd. | 04/16/2026SE |
| K252908 | Easydrip Classic Pen Needle; Easydrip Plus Pen Needle; Easydrip Classic Pro Pen Needle…FMI · Special | Sandstone Medical (Suzhou), Inc. | 03/25/2026SE |
| K253047 | PressoneFMI · Traditional | Nipro Medical Corporation | 03/24/2026SE |
| K253622 | Safety Pen NeedleFMI · Traditional | Ningbo Medsun Medical Co., Ltd. | 03/18/2026SE |
More from Ningbo Medsun Medical Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K884628 | Harborin Central Venous CatheterDQR · Traditional | 05/15/1989SE |
| K890518 | Single Lumen S.E.A.-Port Vascular Access SystemLJT · Traditional | 04/21/1989SE |
| K882657 | Harbor S.E.A.-Port Surgical Accessory KitDYB · Traditional | 12/13/1988SE |
| K881884 | Harbor Central Venous CatheterDQR · Traditional | 07/28/1988SE |
| K882190 | S.E.A.-Port(Tm) Vascular Access SystemLJT · Traditional | 06/09/1988SE |
| K880297 | Sea - Port Infusion SetLJT · Traditional | 02/19/1988SE |
Questions and answers
When was Hypodermic Needles, Single Lumen cleared by the FDA?
Hypodermic Needles, Single Lumen (K874414) received a 510(k) decision of Substantially Equivalent on January 14, 1988, 78 days after the submission was received.
What is the product code of K874414?
The FDA product code is FMI – Needle, Hypodermic, Single Lumen, a Class II (moderate risk) device regulated under 21 CFR 880.5570.